(S)-2-Acetamido-3-(4-chlorophenyl)propanoic acid

98%

Reagent Code: #236992
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CAS Number 55478-55-2

science Other reagents with same CAS 55478-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.6709 g/mol
Formula C₁₁H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD09025650
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing biologically active molecules, especially those targeting enzymes involved in viral replication or metabolic disorders. Commonly employed in the preparation of renin and HIV protease inhibitors due to its ability to mimic peptide bonds and interact selectively with enzyme active sites. Also utilized in asymmetric synthesis to introduce stereochemical control in complex drug molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,360.00
inventory 250mg
10-20 days ฿3,990.00
inventory 1g
10-20 days ฿8,090.00
inventory 5g
10-20 days ฿36,720.00
(S)-2-Acetamido-3-(4-chlorophenyl)propanoic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing biologically active molecules, especially those targeting enzymes involved in viral replication or metabolic disorders. Commonly employed in the preparation of renin and HIV protease inhibitors due to its ability to mimic peptide bonds and interact selectively with enzyme active sites. Also utilized in as

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing biologically active molecules, especially those targeting enzymes involved in viral replication or metabolic disorders. Commonly employed in the preparation of renin and HIV protease inhibitors due to its ability to mimic peptide bonds and interact selectively with enzyme active sites. Also utilized in asymmetric synthesis to introduce stereochemical control in complex drug molecules.

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